We are seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position involves handling and processing adverse events from all sources, including clinical trials and post-marketing surveillance. This role offers a fantastic opportunity to use your previous expertise and further develop your career.
Responsibilities:
- Develop action plans for incoming safety-related calls.
- Collect, process, and track adverse and serious adverse events.
- Write detailed safety narratives.
- Report various safety data.
- Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Qualifications:
- Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, or Pharmacology.
- Preferred: Clinical experience or experience in Clinical Research, case processing, and Post-Marketing Pharmacovigilance.
- Proficient in English.
- Strong knowledge of Microsoft® Office.
- Broad knowledge of medical terminology.
- Strong organizational and communication skills.